and in the worldff

U wastewater treatment and in the worldff. Donald E. Schwinn. Stearns & Wheler, Cazenovia, N.Y. 13035. George K. Tozer. Metcalf & Eddy, Inc., Boston, ...
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FEATURE When completed and with more advanced wastewater treatment processes than any other facility, the Blue Plains plant in Washington, D. C., easily wins the title of the . . . .

'qBrClest advanced U

wastewater treatment and in the worldff Donald E. Schwinn Stearns & Wheler, Cazenovia, N.Y. 13035

George K. Tozer Metcalf & Eddy, Inc., Boston, Mass. 02,716

In June 1968, the District of Columbia (D.C.) retained Metcalf & Eddy (Boston, Mass.) to examine the District's Blue Plains Water Pollution Control Facility. The study, completed in February 1969, recommended the immediate expansion of additional secondary treatment facilities to remove 90% of biological oxygen demand (BOD) and suspended solids (SS), for an average flow of 309 mgd, with provisions for future expansion to 419 mgd and for nutrient removal. These provisions, requiring reclamation of 51 acres of Potomac River mud flats, raised opposition from the Department of Interior at the April 1969 Potomac River Enforcement Conference (PREC). After several months of debate, the Department of Interior and the local jurisdictions signed an agreement limiting the site capacity to 309 mgd .and calling for a second regional plant in suburban Maryland. The 1969 PREC established treatment requirements among the strictest in the nation. The conference proceedings incorporated an implementation schedule for completion of the entire project, including nutrient removal, by 1977. However, in 1970, the Department of Interior requested a construction schedule to provide that all facilities be in operation by December 31, 1974. To meet this schedule, it was essential that all processes for secondary and advanced wastewater treatment be selected by July 1971 and that the design of all facilities be completed by October 1972. 892

Environmental Science & Technology

In 1970, the joint Environmental Protection AgencyDistrict of Columbia (EPA-DC) pilot plant located at the Blue Plains Water Pollution Control Plant was significantly expanded to permit the evaluation of a number of new secondary and advanced treatment methods potentially applicable to meet the new Potomac River criteria. In July 1971, Metcalf & Eddy recommended and the District of Columbia adopted the modified-aeration activated sludge process, upgraded to near 90% BOD and SS removal by the addition of alum or ferric chloride. Other recommendations included: nitrogen removal by the biological nitrification-denitrification process, consisting of nitrification and denitrification reactors and sedimentation basins phosphorus removal by the addition of alum and/or ferric chloride to both the secondary modified aeration system and to the denitrification system; filtration and disinfection of the effluent from the denitrification system before discharge to the river sludge processing by gravity thickening of primary and stormwater sludges, flotation thickening of secondary and advanced treatment sludges, followed by vacuum filtration and incineration. Selection of these key process steps in July 1971 was based on a composite of testing at several locations in the U.S., but the system had not been piloted in its entirety in D.C. Since then, the design has proceeded concurrently with confirmatory tests at the EPA-DC Pilot Plant on D.C. wastewater. This testing program not only demonstrated the high reliability of the recommended processes, but also provided valuable information on design and operating features which have been incorporated into the project.

Implementation progress Because of the subsequent delays in authorization of grant funds, completion of construction, originally scheduled for December 31, 1974, has been delayed until 1978. The project, with an estimated cost of $360 million has been subdivided into approximately 20 contracts. Detailed engineering design of plant components has been divided into several parts, with Metcalf & Eddy responsible for the design of the liquid treatment fac Whitman-Requardt Associates (Baltimore, Md.) for the solids processing facilities. Since three years were originally anticipated to complete the entire $360 million project, it was decided to perform all excavation and site preparation in a single contract, rather than as part of each individual contract. This contract included the excavation of 3.5 million yd3 of material, and dewatering and partial sheeting of the site. The excavation has been fully completed. In February 1972, bids were received for interim chemical feed facilities to feed either ferric chloride or alum to the existing modified activated sludge secondary es for reduction of load on the river while the new facilities were being designed and constructed. The PREC's request, that these facilities be in operation by May 1972, was fulfilled with significant improvement in effluent quality. Construction of additional primary treat-

ment facilities to expand peak capacity from 300 mgd to 939 mgd was corripleted this August. During the initial construction planning phase, Metcalf & Eddy recommended that D.C. build a large docking facility to facilitate shipment of bulk construction materials and equipment. 'This dock would be used for receiving bulk shipments of chemicals and for removal of sludge ash when construction is completed. Accordingly, Metcalf & Eddy designed a docking facility for which construction is now complete. The dock is 1200 X 100 ft, consisting of prestressed concrete slabs. I t is a freestanding structure and can accommodate a concrete plant. Piping is included to receive shipments of chemicals such as alum, ferric chloride, methanol, and fuel oil. A channel has been dredged to the dock site, a distance of approximately ;!OOO ft. For the construction phasing process to permit operation of the new secondary facilities by the fall of 1974, an interim secondary effluent conduit contract was awarded. Bids for construction of additional secondary treatment facilities were opened in December of 1972. Construction is now under way and includes modifications to the existing secondary system, and construction of new secondary reactors ancl sedimentation basins. Completion date for this contract is set for July 1975. Design of instrumentation systems for both primary and secondary treatment facilities has been completed and the construction contract will be awarded in the fall of this year. Bids were opened recently for the multimedia filtration facility substructure and outfall contract. Work under this contract will include construction of the chlorine contact tanks together with an outfall conduit to carry chlorinated effluent to the Pcltomac River. The outfall portion of the

Figure 1

contract is to be completed by July 1975 to permit early operation of the new secondary facilities. The remaining portion of the contract is scheduled to be completed by January 1976. Construction of the solids processing building structure is now completed. Bids have been taken for the sludge dewatering facility. The incineration facilities contract is being reviewed by EPA prior to being let for bids. Design of the chemical building to house the bulk storage facilities for chemicals (ferric chloride, alum, and polymers) has been completed and the contract awarded last winter. The designs for the nitrification reactors, nitrification sedimentation basins, nitrification blower building, and the lime-handling facilities have been done. Construction of these will be completed by the fall of 1976. Design of the denitrification reactors, nitrogen release tanks, and denitrification sedimentation basins has been completed. Funds for these contracts have not yet been appropriated. Design ot the multimedia filter and control facilities was completed last summer. Funds for construction of this phase of the project have not yet been allotted. Instrumentation for the advanced waste treatment facilities is under design. Treatment D.C. s sewage program requires that all combined sewage flows up to two times the dry weather flow receive complete treatment, and that the excess between two times and five times the dry weather flow receive primary treatment and disinfection. All flows from the sanitary portion of the sewer system are to receive complete treatment and will be kept separate from flows emanating from the combined portion of the sewer system.

'p ' CF

Profile of pollutants

Alum or Ferric chloride

Influent -b

PGlw

Nitrification

Secondary

Filtrr:on

Denitrification

Effluent

Disinfection

Pollutant Concentrations: MG/L

BOD,

206

35

10

6

4

8.4

2.0

1.0

0.5

0.2

Organic

8.6

3.0

1.o

1.o

0.5

NH,-N

13.7

14.8

1.5

1.0

1.0

0

0.2

11.1

1.0

0.5

22.3

18.0

13.6

3.0

2.0

Phosphorus,total Nitrogen

NO, & NO3- N Total N

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Figure2

Primary and secondary systems

Alt.

CI 2 Disinfection

Anacostia Force main

-------b Excess flow to river

1

I I Alt. to Filters Or Outfall

Nitrification Influent

I

Legend Continuous intermittent Flow Flow Sludge Wastewater Chemicals (Inc. air)

-- ---

I LCI, I-- Polymer

---

Secondary treatment This system will employ the modified activated sludge process with the addition of alum and/or ferric chloride to achieve a first-stage phosphorus removal of about 70%. Approximately two thirds of the total dose of metal salt will be added at this point. It will be possible to add alum to any reactor and ferric chloride to the remainder for experimental purposes, or if an insufficient supply exists for a single chemical. The modified activated sludge process effluent, enhanced by the addition of alum or ferric chloride, has proved to provide an excellent feed to a biological nitrification system. Because the process operates with very short sludge age, essentially no nitrates are produced, resulting in a more uniform ammonia concentration to the nitrification system and giving more satisfactory control of the nitrification reaction. In addition, the residual metal ions in the secondary effluent appear to improve the settling characteristics of the nitrifying sludge.

Environmental Science & Technology

Or

Ferric or alum

Primary treatment Prior to the expansion program, raw wastewater was pumped to four aerated grit chambers and then discharged to 16 circular primary sedimentation tanks. These facilities had a maximum hydraulic capacity of approximately 300 mgd. Parallel new primary treatment facilities to handle the additional 350 mgd to receive complete treatment and the 289 mgd excess flow needing primary treatment have recently been completed. Dilute sludge from the primary tanks is pumped to six covered existing gravity thickening tanks. Although it is not expected that chemicals need be added to the raw wastewater. flexibility has been provided to allow the addition of a polymer and/or metal salt ahead of the primary sedimentation tanks.

894

Alt. to Nitrification

+ Denitrification WSL To flotation thickeners Operation of the EPA-DC pilot plant has indicated that 90% BOD removals are not required ahead of the nitrification process. However, it appears that the BOD concentration leaving the secondary system should be maintained below 50 mg/l. to ensure satisfactory nitrification. The modified activated sludge process with metal salt addition can consistently meet this requirement. From a cost standpoint, benefits of the metal salt addition are maximized by virtue of the increase in BOD removal efficiency from 75% without chemical to 85% with chemical. Other advantages of the modified activated sludge process are the low oxygen requirements which minimize additional blower requirements, and the low recycle rate which lends itself to obtaining maximum wastewater flow through the existing mixed liquor channels. In contrast to the sludge-bulking problems encountered at the EPA-DC pilot plant for other air and oxygen processes. the modified aeration process has consistently produced a rapidly settling sludge not subject to filamentous growths. Two additional secondary reactors are being added. The existing spiral flow-air diffusion system will be replaced by a stainless steel coarse-bubble diffusion system. The system has been designed to meet the maximum 4-hr oxygen demand at MLVSS concentrations up to 1200 mg/l. to ensure a sufficiently low BOD concentration to the nitrification system during winter conditions. The return sludge system is designed for approximately 10% recycle at peak flow. Separate systems are provided to transfer sludge and scum to flotation thickening tanks. Nitrification/denitrification

The nitrification system will employ plug-flow suspended growth reactors with sedimentation and return sludge facilities. Lime will be added to the nitrification reactor influent to offset reductions in alkalinity caused by up-

stream metal salt addition and to provide sufficient buffer capacity to compensate for the production of nitrates. The five-stage nitrification reactors will be 30 ft deep due to limited space. Each stage will be equipped with two turbine aerators. These units were selected because of the need to ensure adequate mixing while operating under widely varying oxygen demands and wide variations in nitrification rates resulting from seasonal wastewater temperature changes. The hydraulics of the reactors are such that the peak flow can be handled by eight of the 12 reactors to permit the shutting down of four reactors during the summer when nitrification rates are favorable. Turbine aerators and the air distribution system are also designed to meet maximum oxygen demands in eight operating reactors. TABLE 1

Raw wastewater characteristics and edf Iuent r eq u ir e ments Pollutant

BOD Phosphorus (as P) Nitroaen (ToFal as N)

Equivalent removal efficiency,

Influent, Ibldaya

Effluent, Ibfdaya

531,000 21,600

12,700 560

97.6 97.4

57,500

6,130

89.3

1

%

a Based on 309 rngd average annual flow.

Pilot plant work has shown that the residual alum in the secondary effluent and the inert solids from the addition of lime will result in a sludge of approximately 60% volatiles. The system, although designed for an MLSS of 2750 mg/l., has shown itself to be capable of operating at concentrations of 3500-4000 mg/l. However, in the winter months, nitrification sludge settling rates at 4000 mg/l. are approximately one half those at 2750 mg/l. Experience has indicated that denitrification and rising sludge in the nitrification sedimentation basins do not occur because of extremely low carbon concentrations available in the nitrification reactor effluent. Hence, no special facilities for rapid removal of sludge are provided. Waste sludge pumping facilities have been provided to permit periodic MLSS concentration adjustments. Flexibility has been provided to allow the introduction of waste sludge from the modified activated sludge and denitrification processes for seeding and weighing purposes. I t is essential that the effluent from the nitrification

system be as low in dissolved oxygen as possible to minimize methanol demands in the denitrification system. A continuous monitoring system for dissolved oxygen will be provided. Flexibility to add polymer to the nitrification reactor effluent has been provided. Pilot plant tests indicate that the introduction of a small quantity of anionic polymer will enhance the settling properties of the sludge. Although it is not anticipated that polymer addition will be necessary, this back-up feature will provide improved reliability. The effluent from the nitrification sedimentation basins will flow to a low-lift pumping station where it will be lifted to the denitrification system. The denitrification system will employ covered plugflow suspended growth reactors, nitrogen release tanks, and sedimentation basins. Methanol will be added to the reactor influent flow whereas alum or ferric chloride will be added to the nitrogen release tanks for removal of remaining phosphorus. The volume of the denitrification reactors has proved to be significant. Initial sizing studies indicated that a volume of approximately 3.5 million ft3 would be adequate to treat maximum nitrate quantities at minimum temperature. However, pilot plant results in the winter of 1972 indicated that a doubling of reactor volume would be necessary. Because of limited space, it was necessary to increase the depth of the reactors to about 45 ft. The denitrification reactors and return sludge system have been hydraulically designed to permit the operation of four of the eight reactors in the summertime when wastewater temperatures and denitrification rates are favorable. Four nitrogen release tanks will be provided. These tanks are designed to perform several functions: removal of any supersaturated nitrogen gas to avoid rising sludge problems in the sedimentation basins, providing a mixing zone for the addition of alum and for polymer, if necessary, and providing an additional aeration period for the removal of excess methanol. The nitrogen release tanks have been designed to permit the entire peak flow to be passed through two tanks. The design of the 22 denitrification sedimentation basins and sludge recycle and wasting systems will be similar to that employed in the nitrification system. Filtration and disinfection Effluent from the denitrification system will be lifted to a filtration and disinfection building containing 36 multimedia gravity-flow filters and four disinfection tanks. The disinfection tanks will be located beneath the filters. Al-

Figure 3

Ferric or alum

Nitrification and denitrification systems Lime

Polymer

Air

Methanol

Spent Washwater

,Air

I

1

Polymer

Secondary Effluent

legend Continuous Intermittent

- --Flow

Sludge Wastewater WSL To Flotationthickeners

Flow

c . -

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though chlorine can be added either before or after the filters, it is anticipated that continuous chlorine dosing ahead of the filters will be necessary to minimize backwash frequency and to reduce unsightly growths in the filter distribution channels. The filters will be uncovered, located on opposite sides of a central covered gallery. Studies have been conducted at the pilot plant to evaluate various combinations of dual- and trimedia for the filters. The objective of this program was to develop a combination of media which will not require backwashing more frequently than every 12 hr at the 650 mgd peak flow without upstream addition of polymer. Results to date indicate that these criteria can be met by appropriate media selection but that there may be times when the nature of the biological floc will permit only a 6-hr run at peak flow. Consequently, the filter backwash system has been modified to permit a 6-hr backwash interval. If necessary, anionic polymer can be added to the denitrification system to produce an effluent of high quality to permit long filter runs. Filter backwash will be equalized in large conduits located under the filter building prior to return upstream. Flexibility has been provided to return backwash either to the nitrogen release tanks or upstream of the secondary reactors. Normally, the return will be to the nitrogen release tanks. The filtered effluent is collected in two large conduits located between pairs of chlorine contact tanks. Space for future installation of mechanical mixers for chlorine diffusion has been provided in these channels. The disinfected plant effluent will be discharged to the Potomac River. Sludge processing Extensive studies have been completed to determine design data for flotation thickening, vacuum filtration, and incineration. These studies have shown that the chemical and biological sludges from secondary and advanced treatment thicken and dewater at least as well as pure biological sludges from conventional activated sludge systems. The sludge processing building will contain essentially all of the sludge processing components with the exception of the gravity thickening and sludge storage tanks. Other design feature The advanced wastewater treatment facilities are designed to be operated in two halves to permit comparative tests while operating at different MLSS concentrations, chemical dosages, and other variables. Satellite operating laboratories will be provided at key locations in

each treatment system to furnish up-to-the-minute analyses for process control. A s soon as the new sludge processing facilities become available, the existing digestion and elutriation processes can be abandoned. The space occupied by these facilities has been reserved for further treatment should wastewater reuse become a reality. The existing inactive sludge drying and incineration building is being converted to chemical storage facilities. Process instrumentation The treatment plant, when completed, will contain four computer systems, three for process control and one for data processing. One process computer will control the advanced waste treatment system. The other two are for primary and secondary treatment, and for solids processing. The processes that will initially operate with these controls are return sludge, waste sludge, chemical treatment (lime, ferric chloride or alum, methanol, and polymer), and pumping. All process data, equipment status, and alarms will be transmitted to the computers located in Satellite Operations Center (SOC), either as hard-wired electronic signals or multiplexed digital signals from remote data terminals, depending on the number and distance of signal sources to and from the computer center. A s new, more precise, and reliable sensors become available, they can be accommodated within the proposed system as can new software control algorithms relating to process. The influent flow to the secondary reactors will be metered by sonic flow measuring systems and controlled by computer. This system will also be used for pacing the alum or ferric chloride feed systems. The return sludge flow system to the secondary reactors will be provided with a flow regulating system to meter and control the return sludge flow to each reactor. The controls are arranged so that the output from the flow rate controller for any reactor becomes the set point, via ratio units, for the flow controller for the other reactors. A flow-regulating system will also be provided to meter and control the waste sludge flow. The influent flow to the secondary reactors will be provided with a flow-regulating system to meter and control the return sludge flow to each reactor. The controls are arranged so that the output from the flow rate controller for any reactor becomes the set point, via ratio units for the flow controller for the other reactors. A flow-regulating system will also be provided to meter and control the waste sludge flow.

Figure 4

Filtration and disinfection systems Wash Water

4

Spent washwater To nitrogen release Influent channel

Station Polymer

CI

n

+

CI 2 I

I

1

I

Outfall Riverto

Disinfection Tanks

Wastewater Chemicals

896

Legend Continuous Intermittent Flow Flow

-----

Environmental Science & Technology

Sub-cooling Water

Final eff.

Pumps

.

.

&

Flushing, service and Dilutionwater

The influent flow to the secondary reactors will be continuously monitored for phosphate concentration by orthophosphate analyzers. Reactor-dissolved oxygen concentrations will be monitored by each reactor. Mixed liquor will be monitored for pH. Chemical feed pumps for alum or ferric chloride will be controlled by "mass flow" or "pace and trim." "Mass flow" will be the product of secondary influent flow and phosphate concentration and will control pump speed only. "Pacing" will be by influent flow to each reactor to COntrOl pump speed, and "trimming" will be by phosphate concentration to control pump stroke. The pump-pacing control system will include a controller with an integral automatic-manual station, and with remote computer set point capability. For advanced wastewater treatment, a pH monitoring and control system will be provided on the influent flow to the nitrification reactors. The signal will be utilized to trim the lime feed pumps to automatically control the pH. Ammonia and phosphorus analyzers will also be used to monitor the nitrification influent. Mixed liquor SS analyrers will be provided in the first stage of each nitrification reactor. Dissolved oxygen probes will be provided for the nitrification reactors to provide a complete oxygen profile, Two return sludge flow-splitting systems containing six control loops will be provided on the return sludge flow from the nitrification sedimentation basins to the nitrification reactors. Each of the 12 return sludge flow control loops will consist of a rate of flow controller, flow transmitter, and flow indicating controller with remote set point adjustment. A rate of flow metering and control station is provided on the discharge of each of the 42 return sludge pumps. The pump discharge rate will be controlled by manual computer set point control of variablespeed drives on the pumps. Dissolved oxygen analyzers and pH monitoring systems will be provided on the influent flow to the nitrification sedimentation basins. Each sedimentation basin will be equipped with sludge blanket level monitors for highand low-level indication. Two waste sludge metering and control system will be provided on the discharge of the four waste sludge pumps. Each waste sludge metering and control system will meter and control the discharge from either of two waste sludge pumps. Mixed liquor SS analyzers will be provided in the first Stage of each denitrification reactor. A methanol feed pump control system will be provided for pacing of the six methanol pumps in direct relation to the influent flow and nitrate concentration. Ammonia-nitrogen, nitrate-nitrogen, dissolved oxygen, and phosphorus analyzers will be provided for the denitrification reactor influent chan-

nels. The denitrification sludge recycle and wasting systems and their instrumentation and control are similar to that employed in the nitrification system. Ammonia-nitrogen. nitrate-nitrogen, and phosphorus analyzers will be provided to monitor denitrification effluent. A control center will be provided atop the multimedia filtration gallery from which all filters can be controlled. Rather than provide filter consoles at each filter, a communication system has been provided which will permit an operator to monitor backwashing of a filter by relaying directions to the control center. The filter control system will permit automatic sequential backwashing of the filters on the basis of head loss or alternatively at predetermined intervals. A turbidity monitoring system will also be provided for further protection against isolated breakthroughs. SS analyzers will be installed to monitor the filter influent. The filtered effluent will be continuously monitored for pH, dissolved oxygen, ammonia-nitrogen. nitrate-nitrogen. phosphorus, and chlorine residual. When completed, the District of Columbia plant will be the largest advanced wastewater treatment plant in the world. Concurrent design and pilot plant testing have not only saved nearly two years' time but have also resulted in a design which contains a maximum of features proved to be desirable as a result of the testing program. The total project represents a remarkable political, environmental, and technical achievement to clean up a prized water resource.

Donald E. Schwinn is partner of Stearns & Wheler, civil and sanitary engineers, Cazenovia, N. Y. Mr. Schwinn was formerly vice-president and chief, wastewater process engineering of Metcaif & Eddy. i n that position, he was responsible for the pilot plant studies, alternate process evaluations, and process design of the District of Columbia's advanced waste treatment system. George K. Tozer is vice-president of Metcalf & Eddy. Mr. Tozer has more than 20 years' experience in water pollution control engineerina. In the past five years, he has served as project manager for many projects including the 60-mgd secondary treatment plant at Hartford, Conn., as well. as the District of Columbia piant. Coordinated by LCG

-"c

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